9700_w22_qp_22
A paper of Biology, 9700
Questions:
6
Year:
2022
Paper:
2
Variant:
2

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The mammalian circulatory system is adapted for the long-distance transport of the respiratory gases, oxygen and carbon dioxide. The system is described as a closed double circulation. Name: • the two different circulations of the double circulatory system of mammals • the main vein returning deoxygenated blood to the heart. In a closed circulation, blood is kept within vessels at all times. Name the type of blood vessel that connects capillaries and veins. is a diagram of a section through the heart. On : • add a label line and the letter L to show the artery that takes blood from the heart to the lungs • add a label line and the letter R to show the valve that closes when the right ventricle is in systole. The entry of carbon dioxide into red blood cells results in the production of hydrogencarbonate ions. This involves the enzyme carbonic anhydrase. Complete the passage summarising the production of hydrogencarbonate ions by: • writing the correct biological term in the spaces provided • writing the molecular formula for two of the terms in the spaces in brackets. Carbonic anhydrase has an overall spherical shape and is known as a protein. The enzyme acts within the cell so can be described as an enzyme. When blood passes into the capillary network through actively respiring tissues, carbon dioxide (CO2) diffuses into red blood cells and carbonic anhydrase catalyses a reaction where ( ) is combined with CO2 to form (H2CO3), which rapidly forms ions ( ) and hydrogencarbonate ions (HCO3 –).
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Human cytomegalovirus (HCMis a common virus affecting humans. In people with a fully functioning immune system, infection by HCMV usually causes no, or only mild, symptoms. A is a diagram of a section through HCMV. In B, only the outer part of HCMV is sectioned. glycoprotein double-stranded DNA tegument proteins S A B T The viral DNA shown in contains genes that code for proteins important in viral replication and viral structure, including viral DNA polymerase and proteins known as tegument proteins. Viruses can only replicate in host cells as they need to use processes and contents of the host cell. Complete viral particles that are released from the host cell are known as virions. Structure S in A is a subunit of structure T in B. Name the chemical compound used to make structure S and name structure T. S T The actual diameter of the HCMV shown in is 0.17 micrometres (µm). Calculate the actual diameter of the virus in nanometres . Suggest the role of viral DNA polymerase within the host cell. The virus in is drawn as a spherical shape. Structure T is always the same shape. However, electron micrographs show that HCMV virions are not all the same shape. Suggest how HCMV virions can be of different shapes. With reference to A, state one similarity and one difference between the genetic material of HCMV and the genetic material of a typical bacterial cell. HCMV is known to infect some types of human cell that carry out the mitotic cell cycle. Studies have shown that in the presence of one tegument protein, UL69, the cell cycle stops in the G1 stage. Outline the effects the presence of UL69 will have on the normal activity of the mitotic cell cycle. After a person has been infected with HCMV, the virus remains in a dormant state in the body for life. If the virus becomes active again , the virus will only cause serious illness if the person has a weak immune system at that time. Explain why the response to reactivation of HCMV is more likely to cause serious illness in a person who has a weak immune system.
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Plasmodium falciparum is one species of Plasmodium that causes the life-threatening disease malaria. With early diagnosis and the correct drug treatment, the pathogen can be eliminated from the body, particularly if the disease is not severe. Name the type of pathogen that causes malaria. To help prevent the development and spread of drug resistance in Plasmodium, the World Health Organization (WHO) recommends using a treatment known as artemisinin-based combination therapy (ACT). ACT involves two different types of drug: • a fast-acting drug derived from a compound known as artemisinin, which causes a rapid decrease in the number of P. falciparum • one or more longer-acting, non-artemisinin, drugs that eliminate any remaining pathogens. Suggest why using ACT with the two different types of drug is more effective in preventing the development of drug resistance in Plasmodium than a treatment using only one type of drug. In some areas, partial artemisinin resistance has developed. This means ACT takes a longer time for the pathogen to be eliminated from the body. Explain why there is an increased risk of transmission of the pathogen to other people if a person is receiving ACT and the pathogen has partial artemisinin resistance. ACT can act on the stage of the life cycle of P. falciparum that occurs within red blood cells. The cells of P. falciparum in this stage are known as trophozoites. is a photomicrograph of a blood smear (thin layer of cells). Some of the red blood cells contain trophozoites. trophozoite PfK13 is a protein that has an important role in the development of the trophozoite stage of P. falciparum. The gene kelch13 codes for PfK13. Two different mutations of kelch13, known as F446I and C580Y, were investigated to see if they were associated with partial artemisinin resistance. Details of these mutations are summarised in Table 3.1. Table 3.1 name of mutation change in DNA change in protein PfK13 nucleotide present in kelch13 nucleotide present after mutation amino acid before mutation amino acid after mutation F446I thymine (T) adenine (A) phenylalanine isoleucine C580Y guanine (G) adenine (A) cysteine tyrosine Using gene kelch13 and mutation F446I as examples, explain the difference between a gene and a gene mutation. In the investigation, the survival rate of trophozoites within red blood cells was determined for two different concentrations of an artemisinin-based drug known as DHA. Two different strains, A and B, of P. falciparum were tested. Three different cultures of each strain were involved: • no mutation in kelch13 • kelch13 F446I mutation • kelch13 C580Y mutation. Table 3.2 shows the six different cultures tested and the trophozoite survival rate for each culture. Table 3.2 culture number culture details mean percentage survival rate of trophozoite DHA concentration 20 nmol dm–3 DHA concentration 700 nmol dm–3 strain A no mutation 3.15 0.00 strain A, F446I mutation 26.00 0.73 strain A, C580Y mutation 33.08 0.91 strain B no mutation 2.86 0.00 strain B, F446I mutation 13.50 0.53 strain B, C580Y mutation 17.50 0.63 State the main conclusions that can be drawn from the results shown in Table 3.2.
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